Study of Everolimus in the Treatment of Advanced Malignancies in Patients With Peutz-Jeghers Syndrome (EVAMP)
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Purpose
In this pilot study the investigators will treat all patients known with Peutz-Jeghers syndrome (PJS) who are diagnosed with advanced malignancies with everolimus 10mg daily until disease progression. Most patients with PJS have an inherited LKB1 mutation leading to aberrant m-TOR activity. Their risk to develop malignancies or intestinal polyps is probably related to this constitutive mTOR signaling. The hypothesis is that mTOR inhibition is an effective anticancer treatment in PJS patients with advanced malignancies.
| Condition | Intervention | Phase |
|---|---|---|
|
Peutz-Jeghers Syndrome Neoplastic Processes Neoplasm Metastasis |
Drug: Everolimus |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Pilot Study of Everolimus in the Treatment of Neoplasms in Patients With Peutz-Jeghers Syndrome |
- To determine the response rate of Everolimus in patients with advanced cancer and PJS. [ Time Frame: During treatment, expected avarage of 12 months ] [ Designated as safety issue: No ]Determined with regular radiological scans once every 9 weeks and measured following RECIST 1.1
- To determine the overall survival of PJS patients treated with everolimus for advanced malignancies [ Time Frame: avarage of 18 months ] [ Designated as safety issue: No ]The time between date of entering the study and date of death will be collected.
- To determine the time to progression of PJS patients treated with everolimus for advanced malignancies. [ Time Frame: During treatment, expected avarage of 12 months ] [ Designated as safety issue: No ]Determined with regular radiological scans once every 9 weeks and measured following RECIST 1.1
- To determine the safety and toxicity of Everolimus in this patient population [ Time Frame: During treatment, expected avarage of 12 months ] [ Designated as safety issue: Yes ]Number of Participants with Adverse Events determined by the CTCAE 4.0 as a Measure of Safety and Tolerability
- To determine if there is an association between measured drug blood levels and treatment outcome measured as response to treatment determined by RECIST [ Time Frame: During treatment, expected avarage of 12 months ] [ Designated as safety issue: No ]Drug trough levels will be taken once every 3 weeks and stored frozen until measurement at the end of the study
- To assess markers for activated mTOR pathway (including phospho-S6 and phospho-4E BP1) in all pre-treatment tissue specimens and collected specimens during treatment and correlate with response to treatment. [ Time Frame: During treatment, expected avarage of 12 months ] [ Designated as safety issue: No ]All patients who are willing to undergo extra tissue collection will have a tumor and where possible a polyp biopsy before treatment and for tumor biopsy in week 2 and 4 and for polyps once every 6 months during treatment for biomarker investigations. The activity of mTOR and its downstream targets will be measured in the tumor as well as the arborization pattern and apoptosis activity in the polyps.
| Estimated Enrollment: | 15 |
| Study Start Date: | October 2010 |
| Estimated Study Completion Date: | September 2014 |
| Estimated Primary Completion Date: | September 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: afinitor
10mg afinitor daily orally
|
Drug: Everolimus
10mg daily orally
Other Name: Afinitor, RAD001, everolimus
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Tow cohorts of PJS patients will be included. Cohort 1: Advanced malignancy Cohort 2: High risk polyps
General inclusion criteria:
- Known Peutz-Jeghers disease (with LKB1 mutation)
- No concurrent systemic anti cancer treatment
- No prior treatment with m-TOR inhibitor
- Prior malignancies or concurrent second malignancies are allowed
- Prior systemic therapy is permitted with a washout time of at least 4 weeks
- ECOG/ WHO performance 0-2
- Age > 18 years
- Adequate renal function (defined as creatinine < 150 μmol/L)
- Adequate liver function (bilirubin < 1.5 times upper limit of normal, ALAT or ASAT < 5.0 times upper limit of normal in case of liver metastases and < 2.5 the upper limit of normal in absence of liver metastases
- Adequate bone marrow function (WBC > 3.0 x 10 9/L, platelets > 100 x 10 9/L)
- Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial.
- No pregnancy or lactating and ifof childbearing potential patients must agree to use a reliable contraceptive method throughout the study
- No serious concomitant systemic disorder that would compromise the safety of the patient,at the discretion of the investigator
- Signed informed consent according to ICH/GCP.
- No uncontrolled symptomatic hyperglycaemia
Specific inclusion criteria for cohort 1:
- Cytological or histological confirmed carcinoma
- Metastatic or non-resectable disease
- Patients with clinically and/or radiographically documented measurable lesion according to
RECIST criteria:
- X-ray, physical exam > 20 mm
- Spiral CT scan > 10 mm
- Non-spiral CT scan > 20 mm
Specific inclusion criteria for cohort 2:
- Known high risk polyps (definition see page 19)
- Ability to undergo endoscopies
Specific Exclusion criteria:
Symptomatic PJ-polyps, defined as polyps likely to be responsible/causal for the abdominal symptoms the patient presents with.
Contacts and Locations| Contact: Heinz-Josef Klumpen, MD | +31-20-5669111 ext 65955 | h.klumpen@amc.nl |
| Netherlands | |
| Academic Medical Center | Recruiting |
| Amsterdam, Netherlands, 1105AZ | |
| Contact: Eva van Daalen +31205668229 trialmedonc@amc.nl | |
| Principal Investigator: Heinz-Josef Klumpen, MD | |
| Erasmus Medical Center | Not yet recruiting |
| Rotterdam, Netherlands, 3000 CA | |
| Contact: Pieter Dewint, MD, PhD +31.10.7040704 ext 34897 p.dewint@erasmusmc.nl | |
| Contact: Susanne Korsse +31.10.7040704 s.korsse@erasmusmc.nl | |
| Principal Investigator: Pieter Dewint, MD, PhD | |
| Principal Investigator: | Heinz-Josef Klumpen, MD | Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) |
More Information
No publications provided
| Responsible Party: | Heinz-Josef Klumpen, MD, Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) |
| ClinicalTrials.gov Identifier: | NCT01178151 History of Changes |
| Other Study ID Numbers: | AMCmedonc010, 2010-020451-32 |
| Study First Received: | July 26, 2010 |
| Last Updated: | February 12, 2013 |
| Health Authority: | Netherlands: The Central Committee on Research Involving Human Subjects (CCMO) |
Keywords provided by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA):
|
Peutz-Jeghers syndrome mTOR inhibition cancer |
Additional relevant MeSH terms:
|
Neoplasms Neoplasm Metastasis Neoplastic Processes Peutz-Jeghers Syndrome Pathologic Processes Neoplastic Syndromes, Hereditary Intestinal Polyposis Intestinal Diseases Gastrointestinal Diseases Digestive System Diseases Genetic Diseases, Inborn Lentigo Melanosis Hyperpigmentation |
Pigmentation Disorders Skin Diseases Everolimus Sirolimus Immunosuppressive Agents Immunologic Factors Physiological Effects of Drugs Pharmacologic Actions Antibiotics, Antineoplastic Antineoplastic Agents Therapeutic Uses Antifungal Agents Anti-Infective Agents Anti-Bacterial Agents |
ClinicalTrials.gov processed this record on May 23, 2013